関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | p-[4-(Methoxymethylene)cyclohexyl]benzonitrile | HCID 19739357 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(4-Formylcyclohexyl)benzonitrile | HCID 11769829 | 100% |
反応手順
A mixture of 4.2 g of p-[4-(methoxymethylene)cyclohexyl]benzonitrile and 100 ml of tetrahydrofuran/2N hydrochloric acid (vol. 4:1) was heated to reflux for 30 minutes in a round flask. The mixture was subsequently poured into 100 ml of water and extracted three times with 100 ml of diethyl ether each time The organic phases were washed once with 100 ml of water, dried over magnesium sulphate and concentrated There were obtained 3.9 g (100%) of 4-(p-cyanophenyl)cyclohexanecarboxaldehyde as a colourless oil which was used in the next step without further purificarion: trans/cis ratio about 3:1, Rf-value (ethyl acetate/petroleum ether, vol. 3:7) 0.41. By recrystallization from hexane there could be obtained pure trans-4 (p-cyanophenyl)cyclohexanecarboxaldehyde; m.p. 57.1° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04980486 |
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| 出典データセット | uspto-grants-1990_12 |
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| ORD ID | ord-b1a963f121af4e11a3e10c9c616588d7 |
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| 出典メモ | uspto-grants-1990_12 |
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